李福林, 王丽华, 丁德本, 杨俊德, 高徐生. 疟疾治疗药物——4-芳胺基-2-特丁胺甲基酚类化合物的合成J. 药学学报, 1982, 17(1): 77-79.
引用本文: 李福林, 王丽华, 丁德本, 杨俊德, 高徐生. 疟疾治疗药物——4-芳胺基-2-特丁胺甲基酚类化合物的合成J. 药学学报, 1982, 17(1): 77-79.
LI Fu-lin, WANG Li-hua, DING De-ben, YANG Jun-de , GAO Xu-sheng, . STUDIES ON ANTIMALARIALS SYNTHESIS OF 4-ARYLAMINO-TERT-BUTYLAMINOMETHYL PHENOLSJ. Acta Pharmaceutica Sinica, 1982, 17(1): 77-79.
Citation: LI Fu-lin, WANG Li-hua, DING De-ben, YANG Jun-de , GAO Xu-sheng, . STUDIES ON ANTIMALARIALS SYNTHESIS OF 4-ARYLAMINO-TERT-BUTYLAMINOMETHYL PHENOLSJ. Acta Pharmaceutica Sinica, 1982, 17(1): 77-79.

疟疾治疗药物——4-芳胺基-2-特丁胺甲基酚类化合物的合成

STUDIES ON ANTIMALARIALS SYNTHESIS OF 4-ARYLAMINO-TERT-BUTYLAMINOMETHYL PHENOLS

  • Abstract: Six Compounds of 4-arylamino-2-tert-butylaminomethyl phenols have been synthesized and screened for activity against established infections with chloroquine sensitive strain and chloroquine-resistant strains of P. Berghei in mice. All compounds exhibited marked antimalarial effect except compound Ⅳc. Two of these compounds, 4-(7-chloro-4-quinolinylamino)-2-tert-butylaminomethyl-5, 6, 7, 8-tetra-hydro-1-naphthol (compound Ⅳa,) and 4-(2-methoxy-7-chloro-10-benzo-b-1, 5-naphthyridinylamino)-2-tert-butyl-amino-o-cresol (compound Ⅴc)were more effective than the remaining four. The ED50 of compound Ⅳa against infections with chloroquine sensitive strain of P. Berghei was 0.33 mg/kg subcutaneously; the ED50 of compound Ⅴc against infections with chloroquine resistant strain was 1.5 mg/kg. However, the ED50 of chloroquine were 1.12 and 34.5 mg/kg respectively against the 2 strains of P Berghei. Systemetical study of these compounds are in progress.

     

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